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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid

  • CAS No. 914399-98-7

  • Cat. No. CS-0119797
  • Purity≥98%
  • MDL No.MFCD26793609
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    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid|CS-0119797

Structure of 914399-98-7

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Description

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid is a sterically hindered, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group and a tert-butoxy-substituted side chain. This configuration enhances solubility in organic solvents and improves coupling efficiency during solid-phase peptide synthesis. The chiral center at the alpha position ensures enantiomeric purity essential for sequence-specific assembly of biologically active peptides.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid serves as a robust, bench-stable chiral building block for peptide synthesis and heterocyclic scaffold construction. Its tert-butyl ester functionality enables selective deprotection under mild acidic conditions, while the Fmoc group ensures orthogonal protection during multi-step sequences. The sterically hindered α-methyl-α-alkoxy motif enhances diastereoselectivity in coupling reactions and facilitates purification via standard chromatographic methods.

General Information

  • CAS No. 914399-98-7
  • Cat. No. CS-0119797
  • Purity ≥98%
  • MDL No. MFCD26793609
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₃H₂₇NO₅
  • Molecular Weight 397.46
  • Synonym(s) FMoc-α-Me-Ser(tBu)-OH
  • SMILES O=C(O)[C@@](COC(C)(C)C)(C)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O

Computational Chemistry Data

  • TPSA   84.86
  • LogP   4.1835
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   6

Safety Information

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